Knight S J, Flannery A V, Hirst M C, Campbell L, Christodoulou Z, Phelps S R, Pointon J, Middleton-Price H R, Barnicoat A, Pembrey M E
Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, England.
Cell. 1993 Jul 16;74(1):127-34. doi: 10.1016/0092-8674(93)90300-f.
We have cloned the fragile site FRAXE and demonstrate that individuals with this fragile site possess amplifications of a GCC repeat adjacent to a CpG island in Xq28 of the human X chromosome. Normal individuals have 6-25 copies of the GCC repeat, whereas mentally retarded, FRAXE-positive individuals have > 200 copies and also have methylation at the CpG island. This situation is similar to that seen at the FRAXA locus and is another example in which a trinucleotide repeat expansion is associated with a human genetic disorder. In contrast with the fragile X syndrome, the GCC repeat can expand or contract and is equally unstable when passed through the male or female line. These results also have implications for the understanding of chromosome fragility.
我们克隆了脆性位点FRAXE,并证明携带该脆性位点的个体在人类X染色体Xq28区域的一个CpG岛附近存在GCC重复序列的扩增。正常个体的GCC重复序列有6 - 25个拷贝,而智力发育迟缓的FRAXE阳性个体有超过200个拷贝,并且在CpG岛处存在甲基化。这种情况与在FRAXA位点所见的情况相似,是三核苷酸重复序列扩增与人类遗传疾病相关的又一个例子。与脆性X综合征不同,GCC重复序列可以扩增或收缩,并且在通过雄性或雌性系传递时同样不稳定。这些结果对于理解染色体脆性也具有重要意义。